Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
University of Minnesota
Age
21–85
Sex
ALL
Healthy volunteers
Not accepted
You may be eligible if
Male or female ages 21-85 years old with alopecia.
Prospective subjects must be in good general health.
Female subjects who are premenopausal and of childbearing capacity must use oral contraceptive tablets, implanted contraceptive hormones, or Depo-Provera® contraceptive injections as birth control for the duration of the study.
If prospective subjects are on hormone-containing medication, they must be on stable dose for past 6 months.
Willing to abstain from use of over-the-counter hair products such as topical Minoxidil (Rogaine ® ) and prescription hair products.
Willing to use DHS zinc shampoo and conditioner for the duration of the study.
Willing to avoid using any hair styling products directly on the scalp.
Subjects must be capable of giving informed consent.
Willing to adhere to protocol, including scalp examinations, questionnaires, and photography.
Willing to adhere to treatment protocol and frequency used for FDA clearance.
Willing to retain the same hair style and color throughout the duration of the study.
Willing to shampoo/clean scalp at least 3 times per week.
You may not be if
Immunosuppressed patients (history of transplantation, cancer, chemotherapy, splenectomy, or HIV)
Application of topical immunomodulatory or immunosuppressive agent in the preceding 6 weeks.
Systemic administration of corticosteroid or other systemic treatment (i.e., prednisone) that has immunomodulatory or other immunosuppressive mechanisms of action, in the preceding 3 months or planned usage throughout the study.
Clinical evidence of secondary skin infection (i.e., folliculitis).
Other scalp conditions (i.e., seborrheic dermatitis or dissecting cellulitis) that might interfere with evaluations during the study.
Investigational medications within the past 30 days.
Female prospective subject is pregnant, nursing, planning a pregnancy, or less than six months postpartum.
Severe allergies manifested by a history of anaphylaxis, or history or presence of multiple severe allergies.
Use of photobiomodulating device, such as those in this study, within the past 4 weeks
Initiation or change in dose/application of topical minoxidil within the past 6 weeks.
Finasteride or dutasteride within the last 3 months.
Spironolactone within the past 3 months.
Vitamin supplementation (i.e. selenium, or biotin) in excess of daily recommendation per manufacturer.
Lesions in the treated area suspicious for malignancy, or prior skin cancer.
Radiation or chemotherapy to the scalp.
Use of topical or oral ketoconazole in the past 4 weeks.
Hair transplant procedure within the past 6 months or throughout the duration of the study.
History of microneedling procedure performed on scalp.
Changes in hair style while enrolled in the study.
Current weave, or plans to get a weave while enrolled in the study.
Clareo Health | A Clinical Comparison of FDA-Cleared Photobiomodulation Devices for the Treatment of Alopecia
